| Primary Identifier | MGI:2447996 | Allele Type | Transgenic |
| Gene | Sox2 | Inheritance Mode | Recessive |
| Strain of Origin | (CBA x C57BL/6)F1 | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This mutation arose as the result of the random insertion of an unrelated transgene. Molecular analysis indicated that two integration sites had occurred on chromosome 3 and a 20 kb deletion was also associated with one of these integration sites. Genetic noncomplementation tests with a targeted mutation indicated that this mutation is an allele of Sox2. Genomic PCR analysis showed that the coding region and nearby flanking DNA was intact in the mutants. Expression of the gene was severely reduced in the otocyst, in contrast to controls. This tissue specific loss is thought to be due to juxtaposition of the inserted transgenic reporter construct that interferes with the function of tissue-specific regulatory elements. |
